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Cordis Corporation

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K220654 ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture GuidewireNTE2022-04-06 View
510(k) K212977 SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbandsDQO2022-02-17 View
510(k) K210626 SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation CatheterLIT2021-04-23 View
510(k) K202167 Brite Tip Radianz Guiding SheathDYB2021-02-26 View
510(k) K201377 SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation CatheterLIT2020-10-09 View
510(k) K201333 SABER .035 PTA Dilatation CatheterLIT2020-09-11 View
510(k) K181592 RAIN Sheath TransradialDYB2018-08-15 View
510(k) K180081 RAILWAY Sheathless Access SystemDYB2018-04-18 View
510(k) K121442 POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERLIT2012-06-14 View
510(k) K041796 PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEMFGE2004-08-03 View
510(k) K034050 CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220FDTK2004-03-22 View
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